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FDA 510(k)

MARCO LM-770 DIGITAL PROJECTION LENSMETER

K-Number: K930445 · 1993-06-21

ApplicantMarco Ophthalmic, Inc.
Decision Date1993-06-21
Product CodeHLM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MARCO LM-770 DIGITAL PROJECTION LENSMETER is the device name listed in this FDA 510(k) record. The listed applicant is Marco Ophthalmic, Inc.. It received FDA 510(k) clearance on 1993-06-21 under 510(k) number K930445. The device is classified under product code HLM. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARCO LM-770 DIGITAL PROJECTION LENSMETER?

MARCO LM-770 DIGITAL PROJECTION LENSMETER is a medical device that received FDA 510(k) clearance on 1993-06-21. The listed applicant is Marco Ophthalmic, Inc.. The 510(k) number is K930445.

When did MARCO LM-770 DIGITAL PROJECTION LENSMETER receive FDA 510(k) clearance?

MARCO LM-770 DIGITAL PROJECTION LENSMETER received FDA 510(k) clearance on 1993-06-21, under 510(k) number K930445.

Who is the listed applicant for MARCO LM-770 DIGITAL PROJECTION LENSMETER?

The FDA 510(k) record lists Marco Ophthalmic, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARCO LM-770 DIGITAL PROJECTION LENSMETER?

The FDA product code for MARCO LM-770 DIGITAL PROJECTION LENSMETER is HLM.

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Other records listing Marco Ophthalmic, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K943234MS-30 AUTOMATIC PERIMETERK930437MARCO STANDARD RADIUSGAUGESK930444MARCO STANDARD KERATOMETERSK930438MARCO MODELS G,H AND PRIMARY CARE SLIT LAMPSK930442MARCO GXX SERIES PHOTOGRAPHIC SLIT LAMPSK930439MARCO SURGISCOPE OPERATION MICROSCOPES

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Related Devices (Code: HLM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K944022LENSCHEKLeica, Inc.K940997AL-3300Hoya Corp. USAK936199AUTOMATIC LENSOMETERCanon USA, Inc.K930441MARCO STANDARD LENSMETERS 101,201Marco Ophthalmic, Inc.K924785BURTON RADIUSGAUGE - MODEL 2030R.H. Burton Co.K924788BURTON LENSMETERR.H. Burton Co.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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